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Acetylon Pharmaceuticals’ Selective HDAC Inhibitors In Multiple Myeloma, Lymphoma And Sickle Cell Disease And β-Thalassemia To Be Featured In 11 Presentations At The American Society Of Hema­tology Annual Meeting

Published: Nov 25, 2013 9:00 am

Boston (Press Release) - Acetylon Pharma­ceu­ticals, Inc., the leader in the devel­op­ment of selective histone deacetylase (HDAC) inhibitors for en­hanced thera­peutic out­comes, today announced that its selective HDAC inhibitor drug can­di­dates will be the subject of eleven presentations, in­­clud­ing three oral presentations and eight poster presentations of pre­clin­i­cal and clin­i­cal research in multiple myeloma, lym­phoma and sickle cell disease/β-thalassemia at the American Society of Hematology (ASH) Annual Meeting to be held De­cem­ber 7-10, 2013, in New Orleans, LA. The presentations will in­clude interim updates of two clin­i­cal trials of ACY-1215, a selective HDAC6 inhibitor: a Phase 1/2 trial in com­bi­na­tion with bor­tez­o­mib and dexa­metha­sone and a Phase 1b trial in com­bi­na­tion with lena­lido­mide and dexa­metha­sone for the treat­ment of re­lapsed or refractory multiple myeloma. In addi­tion, Acetylon and scientific col­lab­o­rators will present results of pre­clin­i­cal studies of ACY-1215, demonstrating potent com­bi­na­tion treat­ment in disease models of mul­ti­ple mye­lo­ma and lym­phoma, along with pre­clin­i­cal studies of its selective HDAC1/2 inhibitors in sickle cell dis­ease and β-thalassemia.

Details of the presentations are as follows:

Multiple Myeloma
 
Oral Presentation
 
Date: Monday, December 9, 2013
Time: 6:15-7:45pm CT
Location: 393-394
Session: 653. Myeloma: Therapy, excluding Transplantation: Advances in Multiple Myeloma and Plasma Cell Leukemia
Abstract #: 759
Title: ACY-1215, a Selective Histone Deacetylase (HDAC) 6 Inhibitor: Interim Results of Combination Therapy with Bortezomib in Patients with Multiple Myeloma (MM)
 
Poster Presentations
 
Date: Saturday, December 7, 2013
Time: 5:30-7:30pm CT
Location: Hall G
Session: 653. Myeloma: Therapy, excluding Transplantation: Poster I
Abstract #: 1952
Title: ACY-1215, a First-In-Class Selective Inhibitor of HDAC6, Demonstrates Significant Synergy with Immunomodulatory Drugs (IMiDs) in Preclinical Models of Multiple Myeloma
 
Date: Saturday, December 7, 2013
Time: 5:30-7:30pm CT
Location: Hall G
Session: 651. Myeloma: Biology and Pathophysiology, excluding Therapy: Poster I
Abstract #: 1909
Title: Discovery Histone Deacetylase (HDAC)6 Specific Proteomic Biomarkers in Multiple Myeloma (MM) Using Stable Isotope Labeling by Amino Acids in Cell Culture (SILAC)
 
Date: Sunday, December 8, 2013
Time: 6:30-8:30pm CT
Location: Hall G
Session: 653. Myeloma: Therapy, excluding Transplantation: Poster II
Abstract #: 3190
Title: ACY-1215, a Selective Histone Deacetylase (HDAC) 6 Inhibitor, in Combination with Lenalidomide and Dexamethasone (dex), is Well Tolerated Without Dose Limiting Toxicity (DLT) in Patients with Multiple Myeloma at Doses Demonstrating Biologic Activity: Interim Results of a Phase 1b Trial
 
Date: Sunday, December 8, 2013
Time: 6:30-8:30pm CT
Location: Hall G
Session: 653. Myeloma: Therapy, excluding Transplantation: Poster II
Abstract #: 3219
Title: Tubulin Hyper-Acetylation in Blood Lymphocytes: Pharmacodynamic (PD) Biomarker for the Selective Histone Deacetylase (HDAC) 6 Inhibitor ACY-1215 in Multiple Myeloma Patients
 
Date: Monday, December 9, 2013
Time: 6:00-8:00pm CT
Location: Hall G
Session: 652. Myeloma: Pathophysiology and Pre-Clinical Studies, excluding Therapy: Poster III
Abstract #: 4437
Title: Preclinical Combination of the Oral Investigational Agents ACY-1215, a Selective HDAC6 Inhibitor, and Ixazomib, a Proteasome Inhibitor, Demonstrates Combination Benefit in Multiple Myeloma Cell Lines and Xenograft Models
 
Date: Monday, December 9, 2013
Time: 6:00-8:00pm CT
Location: Hall G
Session: 652. Myeloma: Pathophysiology and Pre-Clinical Studies, excluding Therapy: Poster III
Abstract #: 4431
Title: Inhibition of Autophagy by ACY-1215, a Selective HDAC6 Inhibitor, Accelerates Carfilzomib-Induced Cell Death in Multiple Myeloma
 
Lymphoma
 
Oral Presentation
 
Date: Monday, December 9, 2013
Time: 4:30-6:30pm CT
Location: 220-222
Session: 625. Lymphoma: Pre-Clinical – Chemotherapy and Biologic Agents: Small Molecule Targets in Lymphoma
Abstract #: 648
Title: Dual Targeting with the Selective Histone Deacetylase (HDAC) 6 Inhibitor, ACY-1215, and Bortezomib (BOR) Leads to Marked Disruption of Protein Degradation Pathways and Apoptosis in Preclinical Models of Lymphoma
 
Poster Presentation
 
Date: Sunday, December 8, 2013
Time: 6:30-8:30pm CT
Location: Hall G
Session: 625. Lymphoma: Preclinical – Chemotherapy and Biologic Agents: Poster II
Abstract #: 3071
Title: Inhibition of HDAC6 in Combination with Targeted Agents Results in Broad Synergistic Decreases in Viability in Non-Hodgkin’s Lymphoma (NHL) Cells
 
Sickle Cell Disease/β-Thalassemia
 
Oral Presentation
 
Date: Monday, December 9, 2013
Time: 4:30-6:00pm CT
Location: 343-345
Session: 112. Thalassemia and Globin Gene Regulation: Preclinical and Clinical Therapeutic Strategies for Thalassemia
Abstract #: 564
Title: Pharmacological Inhibition of Histone Deacetylase (HDAC) 1, 2 or 3 have Distinct Effects on Cellular Viability, Erythroid Differentiation, and Fetal Globin (HbG) Induction
 
Poster Presentation
 
Date: Sunday, December 8, 2013
Time: 6:30-8:30pm CT
Location: Hall E
Session: 112. Thalassemia and Globin Gene Regulation: Poster II
Abstract #: 2253
Title: Mechanistic Insights into Fetal Hemoglobin (HbF) Induction Through Chemical Inhibition of Histone Deacetylase 1 and 2 (HDAC1/2)
 

About Acetylon

Acetylon Pharma­ceu­ticals, Inc., based in Boston, Massachusetts, is a leader in the devel­op­ment of novel small molecule drugs targeting epigenetic mech­a­nisms for the en­hancement of thera­peutic out­comes in cancer and other critical human diseases. The Company’s epigenetic drug discovery plat­form has yielded a pro­pri­e­tary portfolio of optimized, orally-administered Class I and Class II histone deacetylase (HDAC) selective com­pounds. Alteration of HDAC reg­u­la­tion through selective HDAC inhibition is thought to be appli­­cable to a broad range of diseases in­­clud­ing cancer, sickle cell disease and beta-thalassemia, and auto­immune and neurodegenerative diseases. Acetylon’s lead drug can­di­date, ACY-1215, is a selective HDAC6 inhibitor cur­rently in Phase 1b clin­i­cal devel­op­ment for the treat­ment of multiple myeloma. The Company recently announced a strategic col­lab­o­ration agree­ment with Celgene Corpo­ra­tion, which in­cludes an exclusive option for the future acquisition of Acetylon by Celgene. Acetylon’s scientific founders are affiliated with the Harvard University, the Dana-Farber Cancer Institute, the Massachusetts General Hospital, the Broad Institute and Harvard Medical School. www.acetylon.com

Source: Acetylon Pharma­ceu­ticals.



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